Catalent Pharma Solutions Inc

Group Leader, BioChemical Analysis

Catalent Pharma Solutions Inc$95K — $115K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with over 4 years experience in specific techniques, or a Master's with over 2 years, or a Doctorate with over 1 year.
  • Demonstrated leadership experience, particularly from Catalent-sponsored programs, may be counted in place of external experience.
  • Ability to regularly sit, stand, walk, and occasionally lift up to 40 pounds.
  • Knowledge of principles in Biology, Chemistry, and Biochemistry with familiarity in other scientific areas.
  • Strong project management abilities to handle multiple projects with moderate to high complexity.

Responsibilities

  • Develop, evaluate, and validate analytical methods and conduct stability studies.
  • Plan and execute analytical work per client contracts and technical agreements.
  • Support Project Technical Lead by maintaining project timelines and budgets.
  • Ensure quality of data adherence to SOPs and GMP guidelines.
  • Communicate effectively with clients, auditors, peers, and directors for project execution.
  • Conduct performance reviews and manage HR activities like time approval and salary adjustments.
  • Identify and implement new technologies for enhanced offerings.

Benefits

  • Defined career path with annual performance evaluations.
  • Inclusive company culture promoting diversity.
  • Opportunities for career advancement in a life-improving organization.
  • Generous paid time off including 8 paid holidays.
  • Strong community involvement and environmental initiatives.
  • Day one access to medical, dental, and vision benefits.
  • Tuition reimbursement for continued education.
Full Job Description

Group Leader, BioChemical Analysis

Position Summary

We have an opportunity for a Group Leader, BioChemical Analysis to join our team. In this role, you will manage a sub-team of junior scientists and act as a technical expert on projects. You will serve as a liaison between your team and cross-functional groups, mentor associates, and support client audits and visits. This position plays a key role in analytical activities for Biopharma product development under cGMP regulatory guidance for large molecules and biologics.

Shift: Monday -Friday, 8:00 AM-4:30 PM
Location: Kansas City, MO
100% Onsite

The Role

  • Responsible for method development, evaluation, transfers, verifications, qualifications, validations, stability studies, and ad hoc sample testing.

  • Plan, prioritize, organize, and execute analytical work in accordance with client contracts and technical agreements.

  • Support Project Technical Lead as required, maintaining project timelines and budgets.

  • Ensure integrity and quality of analytical data by adherence to in-house and client SOPs and GMP requirements.

  • Communicate effectively with clients, auditors, peers, and directors to ensure smooth project execution.

  • Carry out performance reviews and HR activities such as time entry approval, PTO approval, and salary adjustments in line with company policy.

  • Identify and implement new technologies with an understanding of their impact on Catalent offerings.

  • All other duties as assigned.

The Candidate

Minimum Requirements

  • Bachelors degree with more than 4 years of relevant experience in department-specific techniques or based on performance at Catalent, OR

  • Masters degree with more than 2 years of relevant experience in department-specific techniques or based on performance at Catalent, OR

  • Doctorate degree with more than 1 year of relevant experience in department-specific techniques or based on performance at Catalent

  • Individual may be required to sit, stand, walk regularly and occasionally lift, pull or push 0-40 pounds.

  • Demonstrable leadership experience at Catalent (including but not limited to participation in Catalentsponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

Preferred Skills & Background

  • Knowledge of principles, theories, and concepts in disciplines such as Biology, Chemistry, and Biochemistry, with broad knowledge in other areas.

  • In-depth knowledge in instrumentation, theory, data interpretation, and applications in at least one technical area, with ability to assess new technologies and their impact on Catalent offerings.

  • Familiarity with most aspects of drug development and lifecycle support, and ability to develop strategies to meet regulatory milestones.

  • Strong project management skills for multiple concurrent projects of moderate to high complexity.

  • High personal credibility, strong motivation skills, and experience in team development.

  • Ability to lead by example in alignment with Catalents values and culture.

Why You Should Join Catalent

  • Defined career path with annual performance reviews and feedback process.

  • Diverse and inclusive culture.

  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.

  • Competitive paid time off plus 8 paid holidays.

  • Community engagement and green initiatives.

  • Medical, dental, and vision benefits effective day one of employment.

  • Tuition reimbursement.

About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Founded
2007

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